Vernessa Pollard advises multi-national life sciences, medical device, and technology companies, helping them navigate US Food and Drug Administration (FDA) regulatory and compliance issues to bring novel technologies and cutting-edge products to market. She provides strategic business and regulatory counsel regarding premarket strategy, including product development, post-market compliance, and regulatory matters that range from manufacturing and quality to advertising and promotion. As a trusted advisor and legal strategist, Vernessa utilizes her years of experience to help clients develop practical, scalable, and innovative strategies for solving challenging regulatory and compliance problems – evaluating risk and achieving business objectives. She previously served as Associate Chief Counsel for Enforcement in the FDA’s Office of Chief Counsel, where she represented the FDA on a variety of regulatory, litigation and enforcement matters.

Upcoming Events:

Past Events

  • Speaker, MedtechVISION 2023 – Driving Inclusive Design as the New Gold Standard
  • Moderator,  MedtechVISION 2018 – Panel 2: The Broader Impact of Regulating AI: Keeping up with innovation in a complex regulatory landscape
Note: Speaker biographies were written at time of speaking engagement and may not reflect their current job title and position.
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